These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


PUBMED FOR HANDHELDS

Journal Abstract Search


122 related items for PubMed ID: 9781029

  • 81.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 82. [On an additional family with dysplasia spondyloepiphysaria tarda].
    Sieweke H.
    Acta Genet Med Gemellol (Roma); 1966 Jan; 15(1):69-78. PubMed ID: 5930173
    [No Abstract] [Full Text] [Related]

  • 83.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 84.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 85. An integrated genetic map of Chromosome 6.
    Cooke IE, Cox SA, Shelling AN, Le Meuth VG, Spurr NK, Ganesan TS.
    Mamm Genome; 1996 Feb; 7(2):157-9. PubMed ID: 8835537
    [No Abstract] [Full Text] [Related]

  • 86. Progressive pseudorheumatoid dysplasia: A rare entity mimicking juvenile idiopathic arthritis.
    Maatallah K, Boussaa H, Lassoued Ferjani H, Kaffel D, Hamdi W.
    Clin Case Rep; 2021 Aug; 9(8):e04670. PubMed ID: 34430024
    [Abstract] [Full Text] [Related]

  • 87. Novel homozygous variant in WISP3 in a family with unrecognized progressive pseudorheumatoid dysplasia.
    Patel C, Khanshour AM, Wilkes D, Rios JJ, Sheff KW, Nassi L, Wise CA.
    Clin Case Rep; 2020 Aug; 8(8):1452-1457. PubMed ID: 32884773
    [Abstract] [Full Text] [Related]

  • 88. Progressive pseudorheumotoid dysplasia: A presentation of four cases with slow and rapid progression and effects of early rehabilitation program.
    Giray E, Yağcı İ, Elçioğlu HN.
    Turk J Phys Med Rehabil; 2019 Sep; 65(3):290-297. PubMed ID: 31663079
    [Abstract] [Full Text] [Related]

  • 89. Novel WISP3 mutations causing progressive pseudorheumatoid dysplasia in two Chinese families.
    Yan W, Dai J, Xu Z, Shi D, Chen D, Xu X, Song K, Yao Y, Li L, Ikegawa S, Teng H, Jiang Q.
    Hum Genome Var; 2016 Sep; 3():16041. PubMed ID: 28018607
    [Abstract] [Full Text] [Related]

  • 90. A homozygous deletion of exon 1 in WISP3 causes progressive pseudorheumatoid dysplasia in two siblings.
    Neerinckx B, Thues C, Wouters C, Lechner S, Westhovens R, Van Esch H.
    Hum Genome Var; 2015 Sep; 2():15049. PubMed ID: 27081554
    [Abstract] [Full Text] [Related]

  • 91.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 92. The genetics of progressive pseudorheumatoid dysplasia (PPRD).
    Yin H, Tang G, Lu L.
    QJM; 2022 Apr 22. PubMed ID: 35451486
    [No Abstract] [Full Text] [Related]

  • 93. The genetics of progressive pseudorheumatoid dysplasia.
    Yin H, Tang G, Lu L.
    QJM; 2022 Apr 22. PubMed ID: 35485200
    [No Abstract] [Full Text] [Related]

  • 94. A Recurrent Biallelic Pathogenic Variant in TBXAS1 Gene Causing Ghosal Hematodiaphyseal Dysplasia.
    Selina A, Kandagaddala M, Madhuri V.
    Indian J Pediatr; 2021 Apr 22; 88(4):381-382. PubMed ID: 33244729
    [No Abstract] [Full Text] [Related]

  • 95. Erratum for: Case 316: Progressive Pseudorheumatoid Dysplasia.
    Gupta A, Bagri N, Chandola S, Jana M.
    Radiology; 2024 Mar 22; 310(3):e249011. PubMed ID: 38530184
    [No Abstract] [Full Text] [Related]

  • 96. Ilizarov technique in an adolescent patient with progressive pseudorheumatoid dysplasia: A case report.
    Xiao K, Li T, Jiang Y, Li Z, Zhu Q, Wu Z, Weng X.
    Medicine (Baltimore); 2018 Aug 22; 97(31):e11375. PubMed ID: 30075503
    [Abstract] [Full Text] [Related]

  • 97. WISP3 mutation associated with pseudorheumatoid dysplasia.
    Sailani MR, Chappell J, Jingga I, Narasimha A, Zia A, Lynch JL, Mazrouei S, Bernstein JA, Aryani O, Snyder MP.
    Cold Spring Harb Mol Case Stud; 2018 Feb 22; 4(1):. PubMed ID: 29092958
    [Abstract] [Full Text] [Related]

  • 98. Ischiopubic and odontoid synchondrosis in a boy with progressive pseudorheumatoid chondrodysplasia.
    Al Kaissi A, Ben Chehida F, Ben Ghachem M, Grill F, Klaushofer K.
    Pediatr Rheumatol Online J; 2007 Sep 27; 5():19. PubMed ID: 17900350
    [Abstract] [Full Text] [Related]

  • 99. Homozygous mutations in LPIN2 are responsible for the syndrome of chronic recurrent multifocal osteomyelitis and congenital dyserythropoietic anaemia (Majeed syndrome).
    Ferguson PJ, Chen S, Tayeh MK, Ochoa L, Leal SM, Pelet A, Munnich A, Lyonnet S, Majeed HA, El-Shanti H.
    J Med Genet; 2005 Jul 27; 42(7):551-7. PubMed ID: 15994876
    [Abstract] [Full Text] [Related]

  • 100. The Impact of Genetic Diseases on Jordanians: Strategies Towards Prevention.
    El-Shanti H.
    J Biomed Biotechnol; 2001 Jul 27; 1(1):45-47. PubMed ID: 12488626
    [No Abstract] [Full Text] [Related]


    Page: [Previous] [Next] [New Search]
    of 7.